We're going to do a little comparison.
I'm going to draw three different people here--
or it could be the same person, I
suppose-- in three different situations.
So you've got the first person just kind of sitting
and maybe they're watching a YouTube video on their laptop.
And you've got a second person who's
actually going for a little walk.
Let's see if I can draw this person walking.
And you've got a third person who's-- let's say this person
is actually really active and they are running.
So they are actually in full stride, running.
And maybe they're late for a test or something.
So-- oh, let me actually change that so their arm does not
look broken.
So there have these three people.
And they're running and walking and sitting, right?
So you can imagine if you were to take a look at their heart
cells they might be doing different things.
In fact, let's draw all three's heart cells
and show you what they might be doing.
So we've got our heart cell.
And in this case I'm actually going to draw also a nerve.
This is going to be the sympathetic nerve.
I'll write an s, for sympathetic nerve.
And the heart cell, just to be clear,
is going to be a ventricular heart cell.
So this is a-- I'll write ventricular heart cell here.
Just so that we know we're not talking about some pacemaker
cell or some other cell in the heart.
This is a ventricular cell.
And now, just to remind us of a couple things we know,
this ventricle cell is branched.
And it's got two little nuclei.
And it's got some receptors on its surface waiting
for, potentially, norepinephrine from that sympathetic nerve.
Right?
Now inside of that heart cell, if we
were to dive inside of the heart cell, you might see some actin.
And you'd see that at the ends of the actin.
It's a Z-disk, right?
So we've got a Z-disk with our actin.
And I've drawn this far too close together.
Let me actually make a little bit of space in here.
But you get the idea.
You've got our actin kind of like little ropes.
And in the middle you've got our myosin.
And our myosin, you remember, is basically
going to have a whole bunch of myosin heads.
And these heads are going to want to do work.
They're going to want to pull the actin
and yank that Z-disk closer to the middle, right?
That's what they want to do.
So these myosins are hanging here, waiting to do work.
And their trigger for work, of course,
is going to be calcium binding the troponin C
and pulling tropomyosin out of the way.
So this is our actin and myosin.
This is our actin up here.
And we've got our myosin in the middle.
And then finally, I'll draw one last thing
and that is the titan.
And the titan, remember, is a protein
that basically is going to attach
the myosin to the Z-disk.
Remember, our Z-disk is this thing at the end.
This is our Z-disk over here.
Let me just kind of draw it in for us.
This right here is our Z-disk.
I've been calling it a Z-disk.
Sometimes you see Z-line.
That's kind of interchangeable.
But this is our Z-disk right here.
And it's basically tethered by those actin ropes,
you can think of them as.
And we're going to use those ropes
to pull the Z-disks together.
So this is basically the set up and what it looks like.
And now I'm actually going to just take this and cut
and paste it a couple of times so that we can actually
use this for our two other situations.
We've got one there.
And we can actually do it again and have it like so.
So now you can see our three situations side
by side and our three setups with our actin, myosin,
and our Z-disks.
So what would happen in situation one?
Well in situation one you're just hanging out.
You're happy.
You're maybe watching something kind of funny on YouTube.
And you don't have much sympathetic drive.
You don't have any stimulation coming
from your sympathetic nerves.
You're not running or you're not frightened, let's say.
So you have-- you know, your normal amount of calcium
comes into the cell when it's time to contract.
And so you get a little bit of calcium in here.
Looking over at the other side, when the calcium comes in,
you have a low amount of calcium, let's say.
Because not much is coming through the channel.
You're not activating that channel in any way.
So that calcium, let's say, it binds here and it binds here.
And let's say a little calcium binds here and here.
And when I say binds remember I mean
it binds the troponin C. Remember that.
So the calcium binds there.
And what do you get?
Well let's draw a little table on the side of-- this is,
let's say, the proportion-- I'm trying
to make sure I phrase it correctly--
the proportion of myosin heads that are working.
And if you count them up, if you count up
all the little purple heads-- you can do that right now--
you'll see there are 20.
So this is the proportion of myosin heads that are working.
And what would you get for this first situation?
Well, at four spots the calcium has bound, right?
And it doesn't bind forever.
At some point the calcium is going
to be kind of taken back into the sarcoplasmic reticulum,
or thrown out of the cell.
But for the time that our heart is contracting,
for that brief bit of time, how many myosin heads are working?
Well we've got this guy over here.
This guy.
And we've got this guy down here.
And we've got this guy and this guy.
So four of them are working.
And that means that 16 are not working.
So 4 out of 20 are working.
So really we've got-- what does that work out to?
20%.
That's equal to 20% of them are working.
So that's not too many.
But what's going to happen?
Basically these myosin heads are going
to pull-- let me erase the little arrows,
not to confuse you.
But basically these myosin heads,
these four that are working, are going
to pull the actin that way and that way.
And this way and this way.
And the Z-disks will come closer together.
Let's not be confused about that point.
The Z-disks definitely will come together.
But it's going to take a while.
Really it's like having four-- you
can think of it as four of your friends pulling on a rope.
It's not as effective as having 20, right?
So let's go to situation number two.
So in situation number two, let's say
now you're going for a walk.
And you're enjoying the beautiful day.
But you're walking, right?
And so there's a little bit of activity.
And so let's say your sympathetics are firing
a little bit, a little bit of a sympathetic drive here.
And a little bit of neurotransmitter gets released.
And so this neurotransmitter, we know, is called norepinephrine.
And so a little bit gets released
into that space between the nerve
and the cell, the heart cell.
And it binds to, let's say, one of the receptors.
So one of the receptors is going to fire.
And during a muscle contraction you've got calcium coming in.
But because that receptor fired now
you have a little bit extra calcium coming in.
Meaning that channel has been activated
so that it's letting more calcium in.
OK so if more calcium's coming in-- let's now take a look
at our diagram.
Now you've got a little bit more calcium coming in and binding.
And I'm just choosing them by random, in a sense.
But let's say these six.
And on this side let's just choose another six.
Let's say four up here and maybe a couple down here
are going to bind calcium.
So you've got troponin C's that are binding calcium.
And of course that means that those
are the myosin heads that get to work.
And so in total, how many myosin heads are working?
Well now instead of only four total,
we've got-- what is that-- 12 myosin heads out
of 20 working, or 60%.
So it's really gone up considerably.
So just as before, you're going to have
the Z-disks getting yanked in.
But now the yanking is going to be much more
forceful because you've got many more myosin heads actually
involved in dragging that Z-disk over.
So this is actually quite interesting
because now you can see that you have,
as a result of the sympathetic drive, more force
in your contraction, your heart contraction.
So you can probably guess where the last one is going to go.
Now you're running.
You're excited.
And let's say, now instead of just a little bit
of transmitter, you've got tons of neurotransmitter being
released, lots and lots of norepinephrine.
In fact, let's say a little bit over here.
And you've got all three receptors kind of firing,
right?
Because all that norepinephrine is
allowing lots and lots of stimulation to the cell.
And so with all this norepinephrine
your calcium channels are going to be really active, right?
They're going to be pouring in calcium.
So instead of just a little bit of calcium,
now when you have a contraction you've
got lots of calcium dumping into the cell, right?
And this is, of course, just during the time
when your contracting or squeezing.
So with all this calcium now it's
going to go and bind the troponin C everywhere
it can find the troponin C. It's going to come and sit
basically everywhere.
And all these myosin heads are excited
because now they all get to work.
And with this full set of myosin heads working--
you have 20 out of 20 working.
You have 100% of them doing their job.
And as a result you can see that now you're
going to have a huge mechanical force, enormous forces,
yanking those Z-disks closer together.
So in all three situations you do
get the Z-disks coming together.
But remember, the period of time that the calcium is
in the heart is finite.
Right?
It's not like it's there forever.
Because, at some point, that calcium's going to get,
as we said, brought back out of the cell
or into the sarcoplasmic reticulum.
So while it's there, for those few precious moments
that the calcium is there, you really
want your heart to be able to do as much work as possible.
And in this case, you're actually
seeing that here at the top-- let's actually
draw an arrow-- at the top this side there's really low energy
use because not too many of the myosin heads
are actually converting ATP to ADP plus phosphate.
So remember, the myosin heads that are working--
those are the only ones that are actually converting ATP
to ADP plus phosphate.
And the ones that are not working
are of course not doing that.
So in this case you can also see that, in addition to force,
the other thing that's less in this sitting situation
is that it's a low-energy state.
You're not really burning any energy.
Whereas over here, when you're running,
each one of these myosin heads is cranking through ATP.
It's making lots and lots of ADP.
So it's using lots of energy.
It's a high-energy situation.
In other words, you're using up a lot of energy here.
And so of course this makes sense.
Right?
Because you think, well if I go for a run of course
I'm going to use up energy.
Whereas if I'm just sitting I'm not using much energy at all.
And now you can see exactly why that's the case.
Because in the running situation, all 20
of your myosin heads are burning through ATP.